C[C@H](O)[C@@H]1[C@H]2[C@@H](C)C(S[C@@H]3C[NH2+][C@H](CNS(N)(=O)=O)C3)=C(N2C1=O)C([O-])=O

InChIKey=AVAACINZEOAHHE-BAMVVWIKSA-N

C15H24N4O6S2

420.5

Organic compounds

Organoheterocyclic compounds

Lactams

Beta lactams

Carbapenems

Thienamycins

Alpha amino acids and derivatives Pyrroline carboxylic acids Azepines Vinylogous thioesters Sulfuric acid diamides Tertiary carboxylic acid amides Quaternary ammonium salts Pyrrolidines Thioenol ethers Tertiary amines Secondary alcohols Amino acids Azetidines Carboxylic acid salts Sulfenyl compounds Azacyclic compounds Monocarboxylic acids and derivatives Carboxylic acids Dialkylamines Carbonyl compounds Organic zwitterions Organic salts Organic oxides Hydrocarbon derivatives

Aliphatic heteropolycyclic compounds

Thienamycin - Alpha-amino acid or derivatives - Pyrroline carboxylic acid - Pyrroline carboxylic acid or derivatives - Azepine - Sulfuric acid diamide - Vinylogous thioester - Organic sulfuric acid or derivatives - Pyrrolidine - Pyrroline - Quaternary ammonium salt - Tertiary carboxylic acid amide - Amino acid or derivatives - Tertiary amine - Secondary alcohol - Thioenolether - Azetidine - Carboxamide group - Amino acid - Carboxylic acid salt - Sulfenyl compound - Azacycle - Carboxylic acid derivative - Carboxylic acid - Secondary aliphatic amine - Monocarboxylic acid or derivatives - Amine - Organic zwitterion - Organic salt - Hydrocarbon derivative - Carbonyl group - Organic nitrogen compound - Organic oxygen compound - Organic oxide - Alcohol - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Aliphatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as thienamycins. These are beta-lactam antibiotics that differ from penicillins in having the thiazolidine sulfur atom replaced by carbon, the sulfur then becoming the first atom in the side chain.

Not available